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791067-32-8

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791067-32-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 791067-32-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,1,0,6 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 791067-32:
(8*7)+(7*9)+(6*1)+(5*0)+(4*6)+(3*7)+(2*3)+(1*2)=178
178 % 10 = 8
So 791067-32-8 is a valid CAS Registry Number.

791067-32-8Downstream Products

791067-32-8Relevant articles and documents

Functional superoxide dismutase mimics. Structural characterization and magnetic exchange interactions of copper(II)-N-substituted sulfonamide dimer complexes

Cejudo-Marin,Alzuet,Ferrer,Borras,Castineiras,Monzani,Casella

, p. 6805 - 6814 (2004)

Dinuclear copper(II) complexes with N-substituted sulfonamide ligands as superoxide dismutase (SOD) mimics have been investigated. The new N-(thiazol-2-yl)toluenesulfonamide (Htz-tol) and N-(thiazol-2-yl)naphthalene- sulfonamide (Htz-naf) ligands have been prepared and structurally characterized. The complexes derived from these ligands, [Cu2(tz-tol)4] (1) and [Cu2(tz-naf)4] (2), have been synthesized, and their crystal structure, magnetic properties, and EPR spectra were studied in detail. In both compounds the metal centers are bridged by four nonlinear triatomic NCN groups. The coordination geometry of the coppers in the dinuclear entity of 1 and 2 is distorted square planar with two N-thiazole and two N-sulfonamido atoms. Magnetic susceptibility data show a strong antiferromagnetic coupling, with -2J = 121.3 cm-1 for compound 1 and -2J = 104.3 cm-1 for compound 2. The EPR spectra of the polycrystalline samples of compounds 1 and 2 have been measured at the X- and Q-band frequencies at different temperatures. Above 20 K the spectra are characteristic of S = 1 species with zero-field splitting parameter D = 0.230 cm-1 for compound 1 and 0.229 cm-1 for compound 2. The EPR parameters are discussed in terms of the known binuclear structures. The complexes exhibit high SOD activity, as shown by the low IC50 values obtained with the xanthine/xanthine oxidase/NBT assay: 0.13 μM for compound 1; 0.17 μM for compound 2.

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